<!DOCTYPE html>
<html>
<head>
    <meta charset="utf-8">
    <meta name="viewport" content="width=device-width, initial-scale=1.0">
    <title>生信结果</title>
    <link rel="shortcut icon" href="favicon.ico">
    <link href="css/bootstrap.min.css?v=3.3.6" rel="stylesheet">
    <link href="css/font-awesome.css?v=4.4.0" rel="stylesheet">
    <!-- Morris -->
    <link href="css/plugins/morris/morris-0.4.3.min.css" rel="stylesheet">
    <!-- Gritter -->
    <link href="js/plugins/gritter/jquery.gritter.css" rel="stylesheet">
    <link href="css/animate.css" rel="stylesheet">
    <link href="css/style.css?v=4.1.0" rel="stylesheet">
    <link href="css/global.css" rel="stylesheet">
    <style>
        .table-striped tbody tr:nth-child(even) {
            background-color: #FAFAFA;
        }
        .table td,.table th{
            height:30px;
            padding: 0;
        }
        .iBoxPagingBox {
            margin-top: .4rem;
        }
    </style>
</head>

<body class="gray-bg">
<div class="wrapper wrapper-content animated fadeInRight">
    <div class="manageTitle">
        <div class="manageTitleBack" onclick="javascript:history.back(-1);">
            <i class="fa fa-chevron-left"></i>
        </div>
        <span class="manageTitleText">生信结果</span>
    </div>
    <div class="ibox float-e-margins">
        <div class="ibox-content">
            <div class="floatClear iboxHeader">
                <div class="iboxheaderTab on">
                    snp.final.2
                </div>
                <div class="iboxheaderTab">
                    indel.final.2
                </div>
                <div class="iboxheaderTab">
                    MIX. snp.final.2
                </div>
                <div class="iboxheaderTab">
                    MIX.indel.final.2
                </div>
            </div>
            <div class="tabContent on">
                <div class="table-responsive" style="font-size: 0;">
                    <div style="display: inline-block; width: 40%; font-size: 12px; padding-bottom: 17px; border-right: 1px solid #ccc;">
                        <table class="table table-striped">
                            <thead>
                            <tr>
                                <th>Chr</th>
                                <th>Start</th>
                                <th>End</th>
                                <th>Ref</th>
                                <th>Alt</th>
                            </tr>
                            </thead>
                            <tbody>
                            <tr>
                                <td noWrap="noWrap">1</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            </tbody>
                        </table>
                    </div>
                    <div style="display: inline-block; width: 60%; font-size: 12px; overflow-x: auto;">
                        <table class="table table-striped" border="0" cellspacing="0" cellpadding="0" style="width: 1000px;">
                            <thead>
                            <tr>
                                <th>Gene.knownGene</th>
                                <th>Func.knownGene</th>
                                <th>GeneDetail.knownGene</th>
                                <th>ExonicFunc.knownGene</th>
                                <th>CDS</th>
                                <th>PEP</th>
                                <th>AAChange.knownGene</th>
                                <th>cytoBand</th>
                                <th>avsnp150</th>
                                <th>Rare_SNP</th>
                                <th>gnomAD_exome_ALL</th>
                                <th>gnomAD_exome_EAS</th>
                                <th>gnomAD_genome_ALL</th>
                                <th>gnomAD_genome_EAS</th>
                                <th>1000g2015aug_all</th>
                                <th>1000g2015_Chinese</th>
                                <th>1000g2015_exac03newALL</th>
                                <th>1000g2015_exac03newEAS</th>
                                <th>1000g2015_CombineWGS</th>
                                <th>1000g2018_CombineWES</th>
                                <th>NovoAF_ALT_AF</th>
                                <th>Interpro_domain</th>
                                <th>anno_DP</th>
                                <th>ALT_RATE</th>
                                <th>MQ</th>
                                <th>anno_het/hom</th>
                                <th>Warning</th>
                                <th>Protein</th>
                                <th>SIFT;Polyphen2_HVAR;Polyphen2_HDIV;MutationTaster;M-CAP;CADD_phred</th>
                                <th>HGMD_All_type</th>
                                <th>snp/indel</th>
                                <th>HGMD;COSMIC</th>
                                <th>AA_type</th>
                                <th>cosmic81</th>
                                <th>CLNDN;CLNHGVS;CLNREVSTAT;CLNSIG</th>
                                <th>CLINVAR_review_status</th>
                                <th>CLINVAR_hgvs</th>
                                <th>CLINVAR_ALLELEID</th>
                                <th>CLINVAR_variation_title</th>
                                <th>CLINVAR_last_evaluated</th>
                                <th>CLINVAR_clinical_significance</th>
                                <th>CLINVAR_condition</th>
                                <th>CLINVAR_supporting_clinvar_record</th>
                                <th>CLINVAR_variant_type</th>
                                <th>CLINVAR_genemic_location</th>
                                <th>CLINVAR_clinical_assertions_citation</th>
                                <th>CLINVAR_summary_evidence_citation</th>
                                <th>CLINVAR_supporting_observations_citation</th>
                                <th>CLINVAR_summary_evidence_description</th>
                                <th>CLINVAR_supporting_observations_description</th>
                                <th>splicing_ada_score;rf_score;dpsi_max_tissue;dps</th>
                                <th>Gene_Symbol</th>
                                <th>HGMD_ID</th>
                                <th>Trans_Num</th>
                                <th>Func</th>
                                <th>Omim_ID</th>
                                <th>Variant</th>
                                <th>Flag</th>
                                <th>cds_ref</th>
                                <th>cds_alt</th>
                                <th>hg19_ref</th>
                                <th>RefUpDown2bp</th>
                                <th>hg19_alt</th>
                                <th>Type_Tag</th>
                                <th>Disease</th>
                                <th>Level</th>
                                <th>Disease_Name</th>
                                <th>Paper</th>
                                <th>Pubmed_ID</th>
                                <th>OMIM_Mim_Number</th>
                                <th>OMIM_Gen_Symbols</th>
                                <th>OMIM_Gene_Name</th>
                                <th>HGNC_ccds_id</th>
                                <th>chr_hg38</th>
                                <th>s_hg38</th>
                                <th>e_hg38</th>
                                <th>ref_hg38</th>
                                <th>alt_hg38</th>
                            </tr>
                            </thead>
                            <tbody>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            </tbody>
                        </table>
                    </div>
                </div>
                <div class="iBoxPagingBox">
                    <div class="iBoxPagingItem"><</div>
                    <div class="iBoxPagingItem on">1</div>
                    <div class="iBoxPagingItem">2</div>
                    <div class="iBoxPagingItem">3</div>
                    <div class="iBoxPagingItem">4</div>
                    <div class="iBoxPagingItem">5</div>
                    <div class="iBoxPagingItem">></div>
                </div>
            </div>
            <div class="tabContent">
                <div class="table-responsive" style="font-size: 0;">
                    <div style="display: inline-block; width: 40%; font-size: 12px; padding-bottom: 17px; border-right: 1px solid #ccc;">
                        <table class="table table-striped">
                            <thead>
                            <tr>
                                <th>Chr</th>
                                <th>Start</th>
                                <th>End</th>
                                <th>Ref</th>
                                <th>Alt</th>
                            </tr>
                            </thead>
                            <tbody>
                            <tr>
                                <td noWrap="noWrap">2</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            </tbody>
                        </table>
                    </div>
                    <div style="display: inline-block; width: 60%; font-size: 12px; overflow-x: auto;">
                        <table class="table table-striped" border="0" cellspacing="0" cellpadding="0" style="width: 1000px;">
                            <thead>
                            <tr>
                                <th>Gene.knownGene</th>
                                <th>Func.knownGene</th>
                                <th>GeneDetail.knownGene</th>
                                <th>ExonicFunc.knownGene</th>
                                <th>CDS</th>
                                <th>PEP</th>
                                <th>AAChange.knownGene</th>
                                <th>cytoBand</th>
                                <th>avsnp150</th>
                                <th>Rare_SNP</th>
                                <th>gnomAD_exome_ALL</th>
                                <th>gnomAD_exome_EAS</th>
                                <th>gnomAD_genome_ALL</th>
                                <th>gnomAD_genome_EAS</th>
                                <th>1000g2015aug_all</th>
                                <th>1000g2015_Chinese</th>
                                <th>1000g2015_exac03newALL</th>
                                <th>1000g2015_exac03newEAS</th>
                                <th>1000g2015_CombineWGS</th>
                                <th>1000g2018_CombineWES</th>
                                <th>NovoAF_ALT_AF</th>
                                <th>Interpro_domain</th>
                                <th>anno_DP</th>
                                <th>ALT_RATE</th>
                                <th>MQ</th>
                                <th>anno_het/hom</th>
                                <th>Warning</th>
                                <th>Protein</th>
                                <th>SIFT;Polyphen2_HVAR;Polyphen2_HDIV;MutationTaster;M-CAP;CADD_phred</th>
                                <th>HGMD_All_type</th>
                                <th>snp/indel</th>
                                <th>HGMD;COSMIC</th>
                                <th>AA_type</th>
                                <th>cosmic81</th>
                                <th>CLNDN;CLNHGVS;CLNREVSTAT;CLNSIG</th>
                                <th>CLINVAR_review_status</th>
                                <th>CLINVAR_hgvs</th>
                                <th>CLINVAR_ALLELEID</th>
                                <th>CLINVAR_variation_title</th>
                                <th>CLINVAR_last_evaluated</th>
                                <th>CLINVAR_clinical_significance</th>
                                <th>CLINVAR_condition</th>
                                <th>CLINVAR_supporting_clinvar_record</th>
                                <th>CLINVAR_variant_type</th>
                                <th>CLINVAR_genemic_location</th>
                                <th>CLINVAR_clinical_assertions_citation</th>
                                <th>CLINVAR_summary_evidence_citation</th>
                                <th>CLINVAR_supporting_observations_citation</th>
                                <th>CLINVAR_summary_evidence_description</th>
                                <th>CLINVAR_supporting_observations_description</th>
                                <th>splicing_ada_score;rf_score;dpsi_max_tissue;dps</th>
                                <th>Gene_Symbol</th>
                                <th>HGMD_ID</th>
                                <th>Trans_Num</th>
                                <th>Func</th>
                                <th>Omim_ID</th>
                                <th>Variant</th>
                                <th>Flag</th>
                                <th>cds_ref</th>
                                <th>cds_alt</th>
                                <th>hg19_ref</th>
                                <th>RefUpDown2bp</th>
                                <th>hg19_alt</th>
                                <th>Type_Tag</th>
                                <th>Disease</th>
                                <th>Level</th>
                                <th>Disease_Name</th>
                                <th>Paper</th>
                                <th>Pubmed_ID</th>
                                <th>OMIM_Mim_Number</th>
                                <th>OMIM_Gen_Symbols</th>
                                <th>OMIM_Gene_Name</th>
                                <th>HGNC_ccds_id</th>
                                <th>chr_hg38</th>
                                <th>s_hg38</th>
                                <th>e_hg38</th>
                                <th>ref_hg38</th>
                                <th>alt_hg38</th>
                            </tr>
                            </thead>
                            <tbody>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            </tbody>
                        </table>
                    </div>
                </div>
                <div class="iBoxPagingBox">
                    <div class="iBoxPagingItem"><</div>
                    <div class="iBoxPagingItem on">1</div>
                    <div class="iBoxPagingItem">2</div>
                    <div class="iBoxPagingItem">3</div>
                    <div class="iBoxPagingItem">4</div>
                    <div class="iBoxPagingItem">5</div>
                    <div class="iBoxPagingItem">></div>
                </div>
            </div>
            <div class="tabContent">
                <div class="table-responsive" style="font-size: 0;">
                    <div style="display: inline-block; width: 40%; font-size: 12px; padding-bottom: 17px; border-right: 1px solid #ccc;">
                        <table class="table table-striped">
                            <thead>
                            <tr>
                                <th>Chr</th>
                                <th>Start</th>
                                <th>End</th>
                                <th>Ref</th>
                                <th>Alt</th>
                            </tr>
                            </thead>
                            <tbody>
                            <tr>
                                <td noWrap="noWrap">3</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            </tbody>
                        </table>
                    </div>
                    <div style="display: inline-block; width: 60%; font-size: 12px; overflow-x: auto;">
                        <table class="table table-striped" border="0" cellspacing="0" cellpadding="0" style="width: 1000px;">
                            <thead>
                            <tr>
                                <th>Gene.knownGene</th>
                                <th>Func.knownGene</th>
                                <th>GeneDetail.knownGene</th>
                                <th>ExonicFunc.knownGene</th>
                                <th>CDS</th>
                                <th>PEP</th>
                                <th>AAChange.knownGene</th>
                                <th>cytoBand</th>
                                <th>avsnp150</th>
                                <th>Rare_SNP</th>
                                <th>gnomAD_exome_ALL</th>
                                <th>gnomAD_exome_EAS</th>
                                <th>gnomAD_genome_ALL</th>
                                <th>gnomAD_genome_EAS</th>
                                <th>1000g2015aug_all</th>
                                <th>1000g2015_Chinese</th>
                                <th>1000g2015_exac03newALL</th>
                                <th>1000g2015_exac03newEAS</th>
                                <th>1000g2015_CombineWGS</th>
                                <th>1000g2018_CombineWES</th>
                                <th>NovoAF_ALT_AF</th>
                                <th>Interpro_domain</th>
                                <th>anno_DP</th>
                                <th>ALT_RATE</th>
                                <th>MQ</th>
                                <th>anno_het/hom</th>
                                <th>Warning</th>
                                <th>Protein</th>
                                <th>SIFT;Polyphen2_HVAR;Polyphen2_HDIV;MutationTaster;M-CAP;CADD_phred</th>
                                <th>HGMD_All_type</th>
                                <th>snp/indel</th>
                                <th>HGMD;COSMIC</th>
                                <th>AA_type</th>
                                <th>cosmic81</th>
                                <th>CLNDN;CLNHGVS;CLNREVSTAT;CLNSIG</th>
                                <th>CLINVAR_review_status</th>
                                <th>CLINVAR_hgvs</th>
                                <th>CLINVAR_ALLELEID</th>
                                <th>CLINVAR_variation_title</th>
                                <th>CLINVAR_last_evaluated</th>
                                <th>CLINVAR_clinical_significance</th>
                                <th>CLINVAR_condition</th>
                                <th>CLINVAR_supporting_clinvar_record</th>
                                <th>CLINVAR_variant_type</th>
                                <th>CLINVAR_genemic_location</th>
                                <th>CLINVAR_clinical_assertions_citation</th>
                                <th>CLINVAR_summary_evidence_citation</th>
                                <th>CLINVAR_supporting_observations_citation</th>
                                <th>CLINVAR_summary_evidence_description</th>
                                <th>CLINVAR_supporting_observations_description</th>
                                <th>splicing_ada_score;rf_score;dpsi_max_tissue;dps</th>
                                <th>Gene_Symbol</th>
                                <th>HGMD_ID</th>
                                <th>Trans_Num</th>
                                <th>Func</th>
                                <th>Omim_ID</th>
                                <th>Variant</th>
                                <th>Flag</th>
                                <th>cds_ref</th>
                                <th>cds_alt</th>
                                <th>hg19_ref</th>
                                <th>RefUpDown2bp</th>
                                <th>hg19_alt</th>
                                <th>Type_Tag</th>
                                <th>Disease</th>
                                <th>Level</th>
                                <th>Disease_Name</th>
                                <th>Paper</th>
                                <th>Pubmed_ID</th>
                                <th>OMIM_Mim_Number</th>
                                <th>OMIM_Gen_Symbols</th>
                                <th>OMIM_Gene_Name</th>
                                <th>HGNC_ccds_id</th>
                                <th>chr_hg38</th>
                                <th>s_hg38</th>
                                <th>e_hg38</th>
                                <th>ref_hg38</th>
                                <th>alt_hg38</th>
                            </tr>
                            </thead>
                            <tbody>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            </tbody>
                        </table>
                    </div>
                </div>
                <div class="iBoxPagingBox">
                    <div class="iBoxPagingItem"><</div>
                    <div class="iBoxPagingItem on">1</div>
                    <div class="iBoxPagingItem">2</div>
                    <div class="iBoxPagingItem">3</div>
                    <div class="iBoxPagingItem">4</div>
                    <div class="iBoxPagingItem">5</div>
                    <div class="iBoxPagingItem">></div>
                </div>
            </div>
            <div class="tabContent">
                <div class="table-responsive" style="font-size: 0;">
                    <div style="display: inline-block; width: 40%; font-size: 12px; padding-bottom: 17px; border-right: 1px solid #ccc;">
                        <table class="table table-striped">
                            <thead>
                            <tr>
                                <th>Chr</th>
                                <th>Start</th>
                                <th>End</th>
                                <th>Ref</th>
                                <th>Alt</th>
                            </tr>
                            </thead>
                            <tbody>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">4</td>
                                <td noWrap="noWrap">86491584</td>
                                <td noWrap="noWrap">7672727</td>
                                <td noWrap="noWrap">C</td>
                                <td noWrap="noWrap">T</td>
                            </tr>
                            </tbody>
                        </table>
                    </div>
                    <div style="display: inline-block; width: 60%; font-size: 12px; overflow-x: auto;">
                        <table class="table table-striped" border="0" cellspacing="0" cellpadding="0" style="width: 1000px;">
                            <thead>
                            <tr>
                                <th>Gene.knownGene</th>
                                <th>Func.knownGene</th>
                                <th>GeneDetail.knownGene</th>
                                <th>ExonicFunc.knownGene</th>
                                <th>CDS</th>
                                <th>PEP</th>
                                <th>AAChange.knownGene</th>
                                <th>cytoBand</th>
                                <th>avsnp150</th>
                                <th>Rare_SNP</th>
                                <th>gnomAD_exome_ALL</th>
                                <th>gnomAD_exome_EAS</th>
                                <th>gnomAD_genome_ALL</th>
                                <th>gnomAD_genome_EAS</th>
                                <th>1000g2015aug_all</th>
                                <th>1000g2015_Chinese</th>
                                <th>1000g2015_exac03newALL</th>
                                <th>1000g2015_exac03newEAS</th>
                                <th>1000g2015_CombineWGS</th>
                                <th>1000g2018_CombineWES</th>
                                <th>NovoAF_ALT_AF</th>
                                <th>Interpro_domain</th>
                                <th>anno_DP</th>
                                <th>ALT_RATE</th>
                                <th>MQ</th>
                                <th>anno_het/hom</th>
                                <th>Warning</th>
                                <th>Protein</th>
                                <th>SIFT;Polyphen2_HVAR;Polyphen2_HDIV;MutationTaster;M-CAP;CADD_phred</th>
                                <th>HGMD_All_type</th>
                                <th>snp/indel</th>
                                <th>HGMD;COSMIC</th>
                                <th>AA_type</th>
                                <th>cosmic81</th>
                                <th>CLNDN;CLNHGVS;CLNREVSTAT;CLNSIG</th>
                                <th>CLINVAR_review_status</th>
                                <th>CLINVAR_hgvs</th>
                                <th>CLINVAR_ALLELEID</th>
                                <th>CLINVAR_variation_title</th>
                                <th>CLINVAR_last_evaluated</th>
                                <th>CLINVAR_clinical_significance</th>
                                <th>CLINVAR_condition</th>
                                <th>CLINVAR_supporting_clinvar_record</th>
                                <th>CLINVAR_variant_type</th>
                                <th>CLINVAR_genemic_location</th>
                                <th>CLINVAR_clinical_assertions_citation</th>
                                <th>CLINVAR_summary_evidence_citation</th>
                                <th>CLINVAR_supporting_observations_citation</th>
                                <th>CLINVAR_summary_evidence_description</th>
                                <th>CLINVAR_supporting_observations_description</th>
                                <th>splicing_ada_score;rf_score;dpsi_max_tissue;dps</th>
                                <th>Gene_Symbol</th>
                                <th>HGMD_ID</th>
                                <th>Trans_Num</th>
                                <th>Func</th>
                                <th>Omim_ID</th>
                                <th>Variant</th>
                                <th>Flag</th>
                                <th>cds_ref</th>
                                <th>cds_alt</th>
                                <th>hg19_ref</th>
                                <th>RefUpDown2bp</th>
                                <th>hg19_alt</th>
                                <th>Type_Tag</th>
                                <th>Disease</th>
                                <th>Level</th>
                                <th>Disease_Name</th>
                                <th>Paper</th>
                                <th>Pubmed_ID</th>
                                <th>OMIM_Mim_Number</th>
                                <th>OMIM_Gen_Symbols</th>
                                <th>OMIM_Gene_Name</th>
                                <th>HGNC_ccds_id</th>
                                <th>chr_hg38</th>
                                <th>s_hg38</th>
                                <th>e_hg38</th>
                                <th>ref_hg38</th>
                                <th>alt_hg38</th>
                            </tr>
                            </thead>
                            <tbody>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            <tr>
                                <td noWrap="noWrap">ARHGAP24</td>
                                <td noWrap="noWrap">intronic</td>
                                <td noWrap="noWrap">nonsynonymous SNV</td>
                                <td noWrap="noWrap">uc010iux.3:c.*1575G>T;uc003jkf.4:c.*1575G>T;uc003jkg.4:c.*1575G>T;uc011cov.2:c.*1575G>T</td>
                                <td noWrap="noWrap">c.*1575G>T</td>
                                <td noWrap="noWrap">p.Tyr63Ser</td>
                                <td noWrap="noWrap">HLA-B:uc010jso.2:exon1:c.G121A:p.E41K,HLA-B:uc021yum.1:exon1:c.G238A:p.E80K,HLA-B:uc003ntf.2:exon2:c.G205A:p.E69K,HLA-B:uc003nth.2:exon2:c.G205A:p.E69K,HLA-B:uc031snl.1:exon2:c.G205A:p.E69K</td>
                                <td noWrap="noWrap">6p21.33</td>
                                <td noWrap="noWrap">rs1071816</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">0.3387</td>
                                <td noWrap="noWrap">MHC</td>
                                <td noWrap="noWrap">52</td>
                                <td noWrap="noWrap">0.83</td>
                                <td noWrap="noWrap">56.86</td>
                                <td noWrap="noWrap">het</td>
                                <td noWrap="noWrap">-</td>
                                <td noWrap="noWrap">-|ALT_rare>0.75</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">Tolerated;Benign;Benign;Polymorphism;.;8.067</td>
                                <td noWrap="noWrap">FALSE</td>
                                <td noWrap="noWrap">snp</td>
                                <td noWrap="noWrap">.;COSMIC</td>
                                <td noWrap="noWrap">0</td>
                                <td noWrap="noWrap">ID=COSM4160817;OCCURENCE=1(thyroid),8(upper_aerodigestive_tract),3(large_intestine)</td>
                                <td noWrap="noWrap">.;.;.;.</td>
                                <td noWrap="noWrap">1 star out of maximum of 4 stars</td>
                                <td noWrap="noWrap">NG_012184.1:g.23155T>C;NM_182548.3:c.*483T>C;NC_000006.12:g.35823448T>C (GRCh38);NC_000006.11:g.35791225T>C (GRCh37)</td>
                                <td noWrap="noWrap">307020</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C Simple - Variation Report - ClinVar - NCBI</td>
                                <td noWrap="noWrap">2016/6/14</td>
                                <td noWrap="noWrap">Likely benign</td>
                                <td noWrap="noWrap">Cryptophthalmos syndrome[MedGen - OMIM] (https://www.ncbi.nlm.nih.gov/medgen/C0265233-http://www.omim.org/entry/219000)</td>
                                <td noWrap="noWrap">NM_182548.3(LHFPL5):c.*483T>C AND Nonsyndromic Hearing Loss, Recessive</td>
                                <td noWrap="noWrap">single nucleotide variant</td>
                                <td noWrap="noWrap">Chr6: 35823448 (on Assembly GRCh38);Chr6: 35791225 (on Assembly GRCh37)</td>
                                <td noWrap="noWrap">GMAF 0.38380 (C)</td>
                                <td noWrap="noWrap">Likely benign (Jun 14, 2016) </td>
                                <td noWrap="noWrap">criteria provided, single submitterICSL Variant Classification 20161018(https://submit.ncbi.nlm.nih.gov/ft/byid/4jQgNGYk/ICSL_Variant_Classification_20161018.pdf)</td>
                                <td noWrap="noWrap">clinical testing</td>
                                <td noWrap="noWrap">Nonsyndromic Hearing Loss, Recessive[MedGen] (https://www.ncbi.nlm.nih.gov/medgen/CN239439)</td>
                                <td noWrap="noWrap">.;.;0.4198;1.045</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">.</td>
                                <td noWrap="noWrap">609427</td>
                                <td noWrap="noWrap">LHFPL5, TMHS, DFNB67</td>
                                <td noWrap="noWrap">LHFP-like protein 5</td>
                                <td noWrap="noWrap">CCDS31960</td>
                                <td noWrap="noWrap">chr6</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">38886385</td>
                                <td noWrap="noWrap">T</td>
                                <td noWrap="noWrap">C</td>
                            </tr>
                            </tbody>
                        </table>
                    </div>
                </div>
                <div class="iBoxPagingBox">
                    <div class="iBoxPagingItem"><</div>
                    <div class="iBoxPagingItem on">1</div>
                    <div class="iBoxPagingItem">2</div>
                    <div class="iBoxPagingItem">3</div>
                    <div class="iBoxPagingItem">4</div>
                    <div class="iBoxPagingItem">5</div>
                    <div class="iBoxPagingItem">></div>
                </div>
            </div>
        </div>
    </div>
</div>

<!-- 全局js -->
<script src="js/jquery.min.js?v=2.1.4"></script>
<script src="js/bootstrap.min.js?v=3.3.6"></script>
<script src="js/global.js?v=3.3.6"></script>
<script>
    $(document).ready(function () {
        //tab切换事件
        $(".iboxheaderTab").click(function(){
            $(".iboxheaderTab").removeClass("on");
            $(this).addClass("on");
            $(".tabContent").removeClass("on").eq($(this).index()).addClass("on");
        });
    });
</script>
</body>
</html>
